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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452377Generated: October 26, 2026

Sodium Thiosulfate → 5-Acetoxy-4,6-di-tert-butylbenzofuran

https://huagongshe.com/reaction/1452377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTrimethylsilyl iodideHCID 85247—
Reactant4-Acetoxy-3,5-di-tert-butyl-2-formylmethylanisoleHCID 10881749—
SolventDichloromethaneHCID 6344—
Product5-Acetoxy-4,6-di-tert-butylbenzofuranHCID 11822332—

Reaction Steps

4-Acetoxy-3,5-di-tert-butyl-2-formylmethylanisole (16 g) was dissolved in dichloromethane (100 ml) and trimethylsilyl iodide (7.1 ml) was added dropwise to the solution under cooling with ice. After stirring the mixture at room temperature for 1 h, a saturated aqueous solution of sodium thiosulfate was added and the mixture was subjected to extraction with chloroform. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 5-acetoxy-4,6-di-tert-butylbenzofuran quantitatively (14.3 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05606089
Source datasetuspto-grants-1997_02
ORD IDord-e86e90d95a5e4978a694c46c5685407a
Source noteuspto-grants-1997_02